Dual-functional probe based on rhodamine for sequential Cu2+ and ATP detection in vivo

被引:34
作者
Jin, Xilang [1 ]
Gao, Jingkai [2 ]
Xie, Pu [1 ]
Yu, Mengchen [3 ]
Wang, Ting [1 ]
Zhou, Hongwei [1 ]
Ma, Aijie [1 ]
Wang, Qian [1 ]
Leng, Xin [4 ]
Zhang, Xianghan [2 ]
机构
[1] Xian Technol Univ, Sch Mat & Chem Engn, Xian 710032, Shaanxi, Peoples R China
[2] Xidian Univ, Sch Life Sci & Technol, Xian 710071, Shaanxi, Peoples R China
[3] Xian Technol Univ, State & Local Joint Engn Lab Adv Network & Monito, Xian 710032, Shaanxi, Peoples R China
[4] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol Chem, Minist Educ, Xian 710069, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Rhodamine; Fluorescence; ATP; Cu2+; Bioimaging; FLUORESCENT-PROBE; LIVING CELLS; LIVE CELLS; MITOCHONDRIA; RECOGNITION; CHEMOSENSOR; DERIVATIVES; FLUOROPHORE; AMINO; HG2+;
D O I
10.1016/j.saa.2018.06.094
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
A rhodamine-based fluorescent probe for Cu2+ and ATP has been designed. The fluorescence intensity/absorbance was significantly enhanced upon the addition of Cu2+ owning to the opening of the Spiro-ring of rhodamine, which quickly returned to the original level due to the reconstruction of the probe by the reacting with ATP. Cu2+/ATP-induced fluorescent intensity/aborbance changes showed a good linear relationship with the concentration of Cu2+/ATP in the range of 2-20 mu M/0-10 mu M with a detection limit of 0.1 mu M/1.0 mu M. The proposed method is simple in design and fast in operation, and is suitable for the reversible monitoring of Cu2+ and ATP in bioanalytical applications. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:657 / 664
页数:8
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